Early effects of nucleus pulposus application on spinal nerve root morphology and function

被引:57
作者
Byröd G. [1 ]
Rydevik B. [1 ]
Nordborg C. [2 ]
Olmarker K. [1 ]
机构
[1] Department of Orthopaedics, Sahlgren University Hospital, Gothenburg University
[2] Department of Pathology, Sahlgren University Hospital, Gothenburg University, Gothenburg
关键词
Inflammation; Mast cells; Nerve function; Nerve roots; Nucleus pulposus;
D O I
10.1007/s005860050106
中图分类号
学科分类号
摘要
It is known that 24 h or more after epidural application of autologous nucleus pulposus, functional and structural changes are established in adjacent nerve roots. It is, however, not known how soon after the application these changes appear. The aim of this study was to reduce the exposure duration to 3 h and to evaluate nerve function and histological changes in the nerve tissue during this time period. A total of 12 pigs was used. In ten pigs, autologous nucleus pulposus (NP) was applied epidurally on the cauda equina. Nerve function was then monitored for 3 h by measurements of muscle action potentials (MAP) in the tail muscles, following nerve root stimulation cranial to the exposed zone. In five of the ten pigs with NP application, nerve root compression to 50 mm Hg was added by means of an inflatable balloon. In two control animals, neither NP nor compression was applied. At the end point, nerve root specimens were harvested for histological assessment. No reduction of MAP amplitude was detected in any of the series. However, there was an epidural accumulation of leucocytes and mast cells, as well as minor axonal and Schwann cell changes in both the NP and NP+ compression series, as compared to the control series. Morphological changes in terms of an epidural inflammatory reaction and minor axonal and Schwann cell damage may thus be demonstrated within 3 h of NP application, with or without compression. However, there is no functional deterioration of the nerve roots detectable within this time period.
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页码:445 / 449
页数:4
相关论文
共 34 条
[1]
Bisla, R.S., Marchisello, P.J., Lockshin, M.D., Hart, D.M., Marcus, R.E., Granda, J., Auto immunological basis of disk degeneration (1976) Clin Orthop, 121, pp. 205-211
[2]
Brenner, T., Soffer, D., Shalit, M., Levi, Schaffer, F., Mast cells in experimental allergic encephalomyelitis: Characterization, distribution in the CNS and in vitro activation by myelin basic protein and neuropeptides (1994) J Neurol Sci, 122, pp. 210-213
[3]
Byröd, G., Otani, K., Larsson, K., Olmarker, K., Rydevik, B., Short term epidural exposure to nucleus pulposus induces increased endoneural capillary permeability and reduction in spinal nerve root blood flow (1997) Eighth Annual Meeting of the European Spine Society, Kos
[4]
Cooper, R.G., Freemont, A.J., Hoyland, J.A., Jenkins, J.P.R., West, C.G.H., Illingworth, K.J., Herniated intervertebral disc associated periradicular fibrosis and vascular abnormalities occur without inflammatory cell infiltration (1995) Spine, 20, pp. 591-598
[5]
Cornefjord, M., Olmarker, K., Rydevik, R., Nordborg, C., Mechanical and biochemical injury of spinal nerve roots: A morphological and neurophysiological study (1996) Eur Spine J, 5, pp. 187-192
[6]
Gertzbein, S.D., Tait, J.H., Devlin, S.R., The stimulation of lymphocytes by nucleus pulposus in patients with degenerative disk disease of the lumbar spine (1977) Clin Orthop, 123, pp. 149-154
[7]
Glynn, L.E., Houck, J.C., Weismann, G., (1984) Cell Biology of Mast Cells and Basophils, , Elsevier/North Holland Biomedical Press, Amsterdam/New York
[8]
Gordon, J.R., Galli, S.J., Mast cells as a source of both preformed and immunologically inducible TNF-alpha/cachectin (1990) Nature, 346, pp. 274-276
[9]
Grönblad, M., Virri, J., Tolonen, J., Seitsalo, S., Kaapa, E., Kankare, J., A controlled immunohistochemical study of inflammatory cells in disc herniation tissue (1994) Spine, 19, pp. 2744-2751
[10]
Hirotaka, H., Kenishi, S., Hiromichi, K., Atsushi, O., Ishiro, S., Nobuyuki, M., Upregulated expression of chemokines in herniated nucleus pulposus resorption (1996) Spine, 21, pp. 1647-1682